Quantitative correlation between susceptibility and OprJ production in NfxB mutants of Pseudomonas aeruginosa

被引:65
作者
Masuda, N [1 ]
Gotoh, N [1 ]
Ohya, S [1 ]
Nishino, T [1 ]
机构
[1] KYOTO PHARMACEUT UNIV,DEPT MICROBIOL,KYOTO 607,JAPAN
关键词
D O I
10.1128/AAC.40.4.909
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Various Pseudomonas aeruginosa PAO1 NfxB mutants were isolated on agar plates containing cefpirome and ofloxacin. They were classified into type A and type B, based on the degrees of changes in their susceptibilities. Type A mutants were four to eight times more resistant to ofloxacin, erythromycin, and new zwitterionic cephems, i,e., cefpirome, cefclidin, cefozopran, and cefoselis, than was the parent strain, PAO1, In contrast, type B mutants were more resistant to tetracycline and chloramphenicol, as well as ofloxacin, erythromycin, and the new zwitterionic cephems, than was PAO1, and they were four to eight times more susceptible to carbenicillin, sulbenicillin, imipenem, panipenem, biapenem, moxalactam, aztreonam, gentamicin, and kanamycin than was PAO1. The changes in susceptibilities of type B mutants were greater than those of type A mutants. The susceptibilities of both type A and type B mutants were restored to the level of PAOI by transformation with plasmid pNF111, which contained the wild-type nfxB gene, demonstrating that they are NfxB mutants, Immunoblot analysis with a monoclonal antibody to OprJ revealed that type B mutants produced larger amounts of outer membrane protein OprJ than did type A mutants and that PAOI produced an undetectable amount of it. Moreover, transconjugants obtained with the different types of NfxB mutants as the donor strains showed almost the same phenotypes as the corresponding donor strains. These results suggest that there are at least two nfxB mutations that show different phenotypes and that production of OprJ is associated with changes in susceptibilities of NfxB mutants.
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页码:909 / 913
页数:5
相关论文
共 28 条
[1]   OUTER-MEMBRANE PERMEABILITY IN PSEUDOMONAS-AERUGINOSA - COMPARISON OF A WILD-TYPE WITH AN ANTIBIOTIC-SUPERSUSCEPTIBLE MUTANT [J].
ANGUS, BL ;
CAREY, AM ;
CARON, DA ;
KROPINSKI, AMB ;
HANCOCK, REW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 21 (02) :299-309
[2]   INVITRO AND INVIVO ANTIBACTERIAL ACTIVITIES OF FK037, A NOVEL PARENTERAL BROAD-SPECTRUM CEPHALOSPORIN [J].
FU, KP ;
FOLENO, BD ;
LAFREDO, SC ;
LOCOCO, JM ;
ISAACSON, DM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (02) :301-307
[3]   NEW NORFLOXACIN RESISTANCE GENE IN PSEUDOMONAS-AERUGINOSA PAO [J].
FUKUDA, H ;
HOSAKA, M ;
HIRAI, K ;
IYOBE, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (09) :1757-1761
[4]   THE OUTER-MEMBRANE PROTEIN OPRM OF PSEUDOMONAS-AERUGINOSA IS ENCODED BY OPRK OF THE MEXA-MEXB-OPRK MULTIDRUG-RESISTANCE OPERON [J].
GOTOH, N ;
TSUJIMOTO, H ;
POOLE, K ;
YAMAGISHI, JI ;
NISHINO, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (11) :2567-2569
[5]   ISOLATION OF OPRM-DEFICIENT MUTANTS OF PSEUDOMONAS-AERUGINOSA BY TRANSPOSON INSERTION MUTAGENESIS - EVIDENCE OF INVOLVEMENT IN MULTIPLE ANTIBIOTIC-RESISTANCE [J].
GOTOH, N ;
ITOH, N ;
TSUJIMOTO, H ;
YAMAGISHI, J ;
OYAMADA, Y ;
NISHINO, T .
FEMS MICROBIOLOGY LETTERS, 1994, 122 (03) :267-273
[6]  
GOTOH N, UNPUB
[7]   MUTATIONS PRODUCING RESISTANCE TO NORFLOXACIN IN PSEUDOMONAS-AERUGINOSA [J].
HIRAI, K ;
SUZUE, S ;
IRIKURA, T ;
IYOBE, S ;
MITSUHASHI, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (04) :582-586
[8]   PURIFICATION OF A 54-KILODALTON PROTEIN (OPRJ) PRODUCED IN NFXB MUTANTS OF PSEUDOMONAS-AERUGINOSA AND PRODUCTION OF A MONOCLONAL-ANTIBODY SPECIFIC TO OPRJ [J].
HOSAKA, M ;
GOTOH, N ;
NISHINO, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (08) :1731-1735
[9]   LOW-COPY-NUMBER AND INTERMEDIATE-COPY-NUMBER CLONING VECTORS BASED ON THE PSEUDOMONAS PLASMID-PVS1 [J].
ITOH, Y ;
SOLDATI, L ;
LEISINGER, T ;
HAAS, D .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY, 1988, 54 (06) :567-573
[10]   INVITRO AND INVIVO ACTIVITIES OF SCE-2787, A NEW PARENTERAL CEPHALOSPORIN WITH A BROAD ANTIBACTERIAL SPECTRUM [J].
IWAHI, T ;
OKONOGI, K ;
YAMAZAKI, T ;
SHIKI, S ;
KONDO, M ;
MIYAKE, A ;
IMADA, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (07) :1358-1366